<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE330nnn/GSE330129/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type> SNP genotyping by SNP array</gds_type><gds_type>Genome variation profiling by SNP array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE330129</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Validation of CNV found by OGM in MDS an t-MN patients</name><description>5 samples to validate ROH in 17p, 2 CNV in RCOR1 gene and 2 CNV in CUX1</description><dates><publication>2026/08/21</publication></dates><accession>GSE330129</accession><cross_references><GSM>GSM9718834</GSM><GSM>GSM9718833</GSM><GSM>GSM9718837</GSM><GSM>GSM9718836</GSM><GSM>GSM9718835</GSM><GPL>36915</GPL><GPL>36916</GPL><GPL>18637</GPL><GSE>330129</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>